Why Choose SCRI

  • Dedicated clinical research site – conducted over 50 Phase I-IV clinical research protocols for multiple sponsors and CROs
  • Recognized as a HIGH ENROLLER in a number of trials in a variety of therapeutic areas
  • High quality data acquisition standards with site specific Standard Operating Procedures
  • Affiliated with multi-therapeutic specialty practice; physicians board certified; access to database of more than 60,000 patients
  • Experienced staff with RN coordinators and certified coordinators, ACRP/SoCRA, average experience > 6 years
  • Board Certified, research-dedicated onsite investigators with more than 50 years of combine clinical research experience
  • Geographic access to over 5 million people
  • Ability to utilize central labs and IRBs
  • Contract relations with Cardiologists, Gastroenterologists, Endocrinologist, Rheumatologist and Radiologists
  • Regulatory Submission and Clinical Trial Agreement turn around time is usually 5 business days